MiMo(TM) Negative Pressure Wound Therapy System
K-Number: K181929 · 2019-03-27
Device Summary
Frequently Asked Questions
What is the MiMo(TM) Negative Pressure Wound Therapy System?
MiMo(TM) Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2019-03-27. It is manufactured by Baymax Research, Inc.. The 510(k) number is K181929.
When was MiMo(TM) Negative Pressure Wound Therapy System approved by the FDA?
MiMo(TM) Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2019-03-27, under approval number K181929.
What company makes MiMo(TM) Negative Pressure Wound Therapy System?
MiMo(TM) Negative Pressure Wound Therapy System is manufactured by Baymax Research, Inc..
What is the FDA product code for MiMo(TM) Negative Pressure Wound Therapy System?
The FDA product code for MiMo(TM) Negative Pressure Wound Therapy System is OMP.
Related Clinical Trials
Related PubMed Literature
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.